Deoxy and deoxyfluoro analogues of acetylated methyl β-d-xylopyranoside––substrates for acetylxylan esterases
作者:Mária Mastihubová、Peter Biely
DOI:10.1016/j.carres.2004.06.001
日期:2004.8
synthesized via 2,3-anhydropentopyranoside precursors. Methyl 2,3-anhydro-4-O-benzyl-beta-D-ribopyranoside was transformed into methyl 2,3-anhydro-4-O-benzyl-beta-D-lyxopyranoside in three steps. The epoxide ring opening of 2,3-anhydropentopyranosides was accomplished either by hydride reduction or hydrofluorination. Methyl beta-D-xylopyranoside 2,3,4-tri-O-, 2,4-di-O-, and 3,4-di-O-acetates, and the prepared
通过2,3合成了乙酰氧基木聚糖酯酶,二-O-乙酰化甲基β-D-吡喃吡喃糖苷的2-脱氧,3-脱氧,2-脱氧-2-氟和3-脱氧-3-氟衍生物的四种修饰底物-脱水戊吡喃糖苷前体。通过三个步骤将甲基2,3-脱水-4-O-苄基-β-D-核吡喃糖苷转化为甲基2,3-脱水-4-O-苄基-β-D-核吡喃糖苷。通过氢化物还原或氢氟化来完成2,3-脱水戊基吡喃糖苷的环氧开环。测试了β-D-吡喃吡喃二甲基2,3,4-tri-O-,2,4-di-O-和3,4-di-O-乙酸酯和制备的二乙酸酯类似物作为乙酰木聚糖酯酶底物的来源裂褶菌公社和里氏木霉。其脱乙酰基速率的测量指出了底物酶的独特结构要求。